• 한국연초학회지
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• 제31권1호
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• pp.39-44
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• 2009

Hydrogen cyanide (HCN) is present in both the particulate and vapor phase of cigarette mainstream smoke. It is one of the 44 harmful substances on Hoffmann's list and is known to be a major ciliatoxic agent in cigarette mainstream smoke. Typically the determination of HCN in cigarette mainstream smoke has been done through colorimetric and electrochemical techniques, such as UV-spectrophotometry (UV), continuous flow analyzer (CFA), ion chromatography (IC) and capillary GC-ECD. In particular, CFA commonly has been using analysis hydrogen cyanide in cigarette smoke and the basic principle is pyridine-pyrazolone reaction. In this study, the more optimized analytical method is suggested isonicotinic acid-pyrazolone reaction method than previous pyridine-pyrazolone reaction method, a commonly used method for the determination of cyanide in water and air, by CFA. Sample collection was optimized by trapping particulate and vapor phase of smoke separately. The optimum NaOH concentration of the trapping solution was shown to be 0.2 M. HCN was stable up to 6 hours in this concentration but only 3 hours in 0.1 M solution. The sensitivity of this method was fairly good and it might be used in analysis of HCN in cigarette mainstream smoke.

• 한국항해항만학회:학술대회논문집
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• 한국항해항만학회 2000년도 추계학술대회논문집
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• pp.73.2-77
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• 2000

해수의 산소요구량(COD; Chemical Oxygen Demand)을 수정진동자로 측정할 수 있는 지의 가능성을 검증하기 위하여 글루코오스 용액에서의 수정진동자의 전기화학적 특성을 조상하였다. 산소요구량을 측정하기 위해서 수정진동자의 표면이 산화되어야 하므로 상대적으로 활성이 있는 금속을 9 MHzAT형 수정진동자의 표면에 코팅하고 일정한 전위를 가할 때 전류와 공진저항의 변화를 조사함으로서 수정진동자의 전기화학적 특성을 조사하였다. 수정진동자는 특별히 제작된 용기에 설치하였고 수정진동자 분석기가 공진주파수와 공진저항의 동시 측정에 사용되었다. 글루코오스의 농도 변화에 따른 측정치의 변화를 관찰하여 농도와 전기화학적 특성의 상관관계를 추적하였다. 이러한 특성조사의 결과 글루코오스 농도가 900 ppm 이하에서는 표준전극 기준 -180mV의 전위가 가해질 때 농도와 초기 최대전류 사이에 직선관계가 있음을 알 수 있었고 이를 이용하면 해수 중 글루코오스 농도를 측정할 수 있으며 글루코오스 농도와 화학적 산소 요구량 사이에 직접적인 관계가 있음을 고려할 때 수정진동자를 이용한 화학적 산소요구량의 측정이 가능함을 알 수 있었다.

• 대한기계학회논문집A
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• 제23권11호
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• pp.2014-2021
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• 1999

The present investigation is concerned with the degradation characteristics of cast stainless steel(CF8M), exposed to the $\sigma$-phase degradation at $700^{\circ}C$. In the present paper, the degradation of CF8 M at $700^{\circ}C$ is evaluated by a non-destructive test, DL-EPR(double loop electrochemical potentiokinetic reactivation). The surface of specimens is observed by using scanning electron microscopy after DL-EPR test. Also. chromium contents of matrix, grain boundary and ferrite phase are analyzed by electron probe X-ray micro analyzer. Through the experiments, the following results are obtained 1) The degree of sensitization(DOS) of CF8M aged up to 15hr at $700^{\circ}C$ is increased with acing time while that is decreased with aging time from 15hr to 150hr. 2) The impact energy decreases with increase of $\sigma$-phase while DOS increases with $\sigma$-phase until aging time reaches to 15hr. After the aging time. 15hr, the $\sigma$-phase and the rate of impact energy with respect to aging time decreases. Therefore the degradation behavior of the CF8M can be evaluated by comparing SEM micrographs and the value of DOS.

• 전기화학회지
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• 제8권3호
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• pp.130-134
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• 2005

본 연구에서는 그동안 전기화학적으로 합성되지 못했던 III-V족 화합물 반도체 InSb를 구연산 용액으로부터 합성하였으며 자체 제조한 AAO를 나노템플릿으로 이용하여 정전압 도금을 실시하여 InSb 나노와이어를 제조하였다 제조된 InSb나노와이어는 X선 회절분석 결과 단결정의 나노와이어는 아니었으나 정확하게 화학양론을 만족시키는 화합물임을 확인하였고, 평판 박막 상태의 InSb와는 달리 나노와이어의 길이방향으로 (220) 방향의 결정이 주로 성장하는 우선결정방위를 가지고 있음을 알 수 있었다. 또한 집합적으로 배열된 상태에서 측정된 I-V특성 곡선에서는 n형 반도체의 특성을 보이되 밴드갭이 좁고, 전자이동도가 큰 InSb고유의 특성상 반금속과 유사한 전기적 특성을 보유하고 있음을 확인하였다.

• 한국전기전자재료학회논문지
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• 제27권11호
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• pp.725-729
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• 2014

In this study, a transparent conductive oxide (TCO)-less dye-sensitized solar cells (DSSCs) was fabricated by using titanium (Ti) electrode to replace the Fluorine-doped tin oxide (FTO) for the reduction of manufacturing cost. Ti film was formed by electron beam evaporation method and the results showed the sheet resistance of Ti electrodes with a thikness of 500 nm similar to FTO. In case of power conversion efficiency (PCE), a DSSC with Ti electrodes showed a lower value than that with FTO by 0.38%. For the investigation of the difference, the DSSCs were measured and analyzed by using electrochemical impedance analyzer (EIS).

• 한국연초학회지
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• 제29권2호
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• pp.125-131
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• 2007

Hydrogen cyanide(HCN), formed from pyrolysis of various nitrogenous compounds such as protein, amino acids and nitrate in tobacco, is present in both the particulate phase and vapor phase of cigarette smoke. Typically the determination of HCN in cigarette smoke has been done through colorimetric and electrochemical techniques, such as fluorescence spectrometry, UV-spectrophotometry (UV), continuous flow analyzer (CFA), capillary GC-ECD and ion chromatography (IC). Most of these techniques are known to be time-consuming and some of them lack specificity or sensitivity. The available results from both our laboratory and reported literatures for 2R4F Kentucky reference cigarette, smoked under ISO condition, show a relatively wide variation ranging from 100 to 120 ug/cig of HCN. Especially, the precision and accuracy of the analytical results of HCN tend to get worse in low tar cigarettes and under intense smoking condition. In this paper, a more optimized analytical methods than previous ones are suggested. This method shows lower detection limit and has improved precision and accuracy, so it is applicable for wide tar level cigarettes under intense smoking condition as well as under ISO smoking condition. Important features of this method are improved sample collection and quantification systems such as the number of trapping units, volume, temperature and type of trapping solution. To avoid volatilization loss of HCN in analyzing mainstream smoke, it is highly recommended that pH values of trapping solutions should be maintained over 11 and cold traps should be used in collecting mainstream smoke.

• Corrosion Science and Technology
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• 제18권6호
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• pp.300-311
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• 2019

The corrosion behaviors of twinning-induced plasticity (TWIP) steels with different alloying elements (Cu, Al, Si) in a neutral aqueous environment were investigated in terms of the characteristics of the corrosion products formed on the steel surface. The corrosion behavior was evaluated by measuring potentiodynamic polarization test and electrochemical impedance spectroscopy. For compositional analysis of the corrosion products formed on the steel surface, an electron probe x-ray micro analyzer was also utilized. This study showed that the addition of Cu to the steel contributed to the increase in corrosion resistance to a certain extent by the presence of metallic Cu in discontinuous form at the oxide/steel interface. Compared to the case of steel with Cu, the Al-bearing specimen exhibited much higher polarization resistance and lower corrosion current by the formation of a thin Al-enriched oxide layer. On the other hand, Si addition (3.0 wt%) to the steel led to an increase in grain size, which was twice as large as that of the other specimens, resulting in a deterioration of the corrosion resistance. This was closely associated with the localized corrosion attacks along the grain boundaries by the formation of a galvanic couple with a large cathode-small anode.

• 전기화학회지
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• 제6권2호
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• pp.130-133
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• 2003

3,4-dihydroxybenzoic acid(3,4-DHBA)를 전기화학법으로 유리탄소 전극 위에 중합하여 GC/p-3,4-DHBA형의 전극을 제작한 후 이 전극을 도파민으로 재 수식한 전극을 제작하였다. 이 때 고분자 피막 상에 카르복시기와 도파민의 아민 기간에 짝 짓기 반응은 1-(3-dimethylaminopropyl)-3-ethyl carbodiimide hydrochloride(EDC)의 존재하에서 진행되었다. 이 반응과정에서 반응한 도파민의 양은 수정판 분석기(quartz crystal analyzer:QCA)에 의하여 결정하였으며 그때 전극형태는 QCA(Au)/p-3,4-DHBA-dopamine이었다. 이 전극의 표면은 o-퀴논부분을 갖고 있어서 티탄이온에 선택성이 큰 특성을 갖고 있다. 이 전극의 산화환원과정은 $hydroquinone = quinone +2H^+2e^-$으로 두 개의 강한 파와 두개의 약한 파가 CV과정에서 관찰되었다. 이 수식전극으로 Ti(IV)이온을 $4.13\times10^{-5} gcm^{-2}$만큼 포집할 수가 있었다. 이 수식 전극으로 $5.25\times10^{-4}M$에서 $5.25\times10^{-8}M$농도범위까지 정량 할 수 있는 상관계수가 0.997인 검정선을 얻었다.

• 전기화학회지
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• 제12권1호
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• pp.34-39
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• 2009

니들 코크스의 활성화를 위해 $HNO_3$와 $NaClO_3$ 혼합용액에서의 산처리와 열처리를 행하였다. 산화처리 코크스와 열처리한 코크스의 미세구조는 XRD, FESEM, elemental analysis, BET, Raman spectroscopy를 이용하였으며, 전기이중층 거동은 충방전 분석을 행하였다. 니들 코크스는 산화처리 시간에 따라 산소의 중량 %의 증가와 함께 층간이 분리되어(001) 구조로 상변화가 일어나고, $200^{\circ}C$ 이상의 열처리에서 흑연구조 특성인(002) 구조로 되돌아갔다. 이들 산화처리 과정에서 층간에 관능기가 도입 되어 구조결함이 발생하고 1차 충전에서 전계 활성화에 의해 층간을 확장되어 2차 충전에서 전기이중층 용량을 발생 시키는 것으로 보인다. 24시간 산화처리후 $300^{\circ}C$ 열처리한 코크스의 2.5 V까지의 2 전극 기준에서 구한 활물질 중량 당 용량과 전극 부피 당 용량은 각각 32.1 F/g과 29.5 F/ml을 나타내었다.

• 대한전기학회:학술대회논문집
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• 대한전기학회 2008년도 제39회 하계학술대회
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• pp.1295-1296
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• 2008

Hydrogen peroxide ($H_2O_2$) biosensor is one of the most developing sensors because this kind of sensors is highly selective and responds quickly to the specific substrate. Hemoglobin (Hb) has been used as ideal biomolecules to construct hydrogen peroxide biosensors because of their high selectivity to $H_2O_2$. The direct electron transfer of Hb has widely investigated for application in the determination of $H_2O_2$ because of its simplicity, high selectivity and intrinsic sensitivity. An electrochemical detection for hydrogen peroxide was investigated based on immobilization of hemoglobin on DNA/Fe(pyterpy)$^{2+}$ modified gold electrode. The pyterpy monolayers were firstly an electron deposition onto the gold electrode surface of the quartz crystal microbalance (QCM). It is offered a template to attach negatively charged DNA. The fabrication process of the electrode was verified by quartz crystal analyzer (QCA). The experimental parameters such as pH, applied potential and amperometric response were evaluated and optimized. Under the optimized conditions, this sensor shows the linear response within the range between $3.0{\times}10^{-6}$ to $9.0{|times}10^{-4}$ M concentrations of $H_2O_2$. The detection limit was determined to be $9{\times}10^{-7}$ M (based on the S/N=3).